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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Striking regression of subcutaneous fibrosis induced by high doses of gamma rays using a combination of pentoxifylline and alpha-tocopherol: an experimental study.
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Striking regression of subcutaneous fibrosis induced by high doses of gamma rays using a combination of pentoxifylline and alpha-tocopherol: an experimental study.

机译:结合己酮可可碱和α-生育酚,大剂量伽马射线引起的皮下纤维化的惊人消退:一项实验研究。

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摘要

PURPOSE: To establish a successful treatment of subcutaneous fibrosis developing after high doses of gamma rays, suitable for use in clinical practice. METHODS AND MATERIALS: We used an animal model of acute localized gamma irradiation simulating accidental overexposure in humans. Three groups of 5 Large White pigs were irradiated using a collimated 192Ir source to deliver a single dose of 160 Gy onto the skin surface (100%) of the outer side of the thigh. A well-defined block of necrosis developed within a few weeks which had healed after 26 weeks to leave a block of subcutaneous fibrosis involving skin and skeletal muscle. One experimental group of 5 pigs was dosed orally for 26 weeks starting 26 weeks after irradiation with 1600 mg/120 kg body weight of pentoxifylline (PTX) included in the reconstituted food during its fabrication, and another group of 5 was dosed orally for the same period with a daily dose of 1600 mg/120 kg body weight of PTX combined with 2000 IU/120 kg body weight of alpha-tocopherol. Five irradiated control pigs were given normal food only. Animals were assessed for changes in the density of the palpated fibrotic block and in the dimensions of the projected cutaneous surface. Depth of scar tissue was determined by ultrasound. Physical and sonographic findings were confirmed by autopsy 26 weeks after treatment started. The density, length, width, and depth of the block of fibrotic scar tissue, and the areas and volume of its projected cutaneous surface, were compared before treatment, 6 and 13 weeks thereafter, and at 26 weeks. RESULTS: The experimental animals exhibited no change in behavior and no abnormal clinical or anatomic signs. No modifications were observed in the block of fibrotic scar tissue of pigs dosed with PTX alone. However, significant softening and shrinking of this block were noted in the pigs dosed with PTX + alpha-tocopherol 13 weeks after treatment started and at autopsy, when mean regression was approximately 30% for length, approximately 50% for width and depth, and approximately 70% for area and volume. Histologic examination showed completely normal muscle and subcutaneous tissue surrounding the residual scar tissue. The 50% decrease in the linear dimensions of the scar tissue, were comparable to the results obtained in our previous clinical studies, and were highly significant compared to the clinical and autopsy results for the controls. Histologic examination of the residual scar tissue revealed tissue which was more homogenous and less cellular and inflammatory than in control and PTX-dosed pigs. The tissular and cellular immunolocalization of tumor necrosis factor alpha (TNFalpha) was similar in the residual fibrotic tissues of all three groups of pigs, whereas the immunostaining of transforming growth factor beta-1(TGFbeta-1) diminished much more in the residual fibrotic scar tissue of the PTX + alpha-tocopherol-dosed pigs than in the two other groups. CONCLUSIONS: The present results showed a striking regression of the subcutaneous fibrotic scar tissue that develops as a consequence of high doses of gamma rays.
机译:目的:建立成功治疗高剂量伽马射线后发展的皮下纤维化的方法,适合在临床上使用。方法和材料:我们使用了急性局部伽马射线辐照的动物模型来模拟人的意外过度暴露。使用准直的192Ir光源辐照三组的5只大白猪,以将160 Gy的单剂量递送至大腿外侧的皮肤表面(100%)。在数周内出现了明确的坏死块,在26周后已愈合,剩下一块涉及皮肤和骨骼肌的皮下纤维化块。实验组5头猪在制作后的过程中,以1600 mg / 120 kg体重的己酮可可碱(PTX)照射后的26周开始,口服26周,另一组5只经同样的剂量口服每天服用1600 mg / 120公斤体重的PTX和2000 IU / 120公斤体重的α-生育酚。仅给五头经辐照的对照猪提供普通食物。评估动物触诊纤维化块的密度和投射的皮肤表面尺寸的变化。疤痕组织的深度通过超声确定。治疗开始26周后通过尸检证实了身体和超声检查结果。比较了治疗前,治疗后6周和13周以及26周时纤维化瘢痕组织块的密度,长度,宽度和深度,以及其投射的皮肤表面的面积和体积。结果:实验动物没有表现出行为改变,也没有异常的临床或解剖体征。单独施用PTX的猪的纤维化瘢痕组织阻滞未见任何改变。但是,在开始治疗后13周和尸检时,在给猪注射PTX +α-生育酚的猪中发现了这种阻滞的显着软化和收缩,当时平均消退的长度约为30%,宽度和深度约为50%,而面积和体积的70%。组织学检查显示残留的瘢痕组织周围的肌肉和皮下组织完全正常。疤痕组织的线性尺寸降低了50%,与我们之前的临床研究结果相当,并且与对照组的临床和尸检结果相比具有显着意义。残余疤痕组织的组织学检查显示,与对照和PTX给药的猪相比,该组织更均匀,细胞和炎症更少。在三组猪的残余纤维化组织中,肿瘤坏死因子α(TNFalpha)的组织和细胞免疫定位相似,而转化生长因子β-1(TGFbeta-1)的免疫染色在残余纤维化瘢痕中减少得更多。与其他两组相比,PTX +α-生育酚给药的猪的组织。结论:目前的结果表明,皮下纤维化瘢痕组织的显着退化是由于高剂量的伽马射线而形成的。

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